Medical Science Liaison (Mid Atlantic)

Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. With several marketed products in the U.S., Canada, and Europe, and a diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website (or follow us on LinkedIn (. Job Summary We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Medical Science Liaison (MSL) . The MSL will be responsible for integrating scientific expertise and knowledge with medical strategies to ensure successful implementation of Sumitomo Pharma Americau2019s marketed and emerging product portfolio. This will be fulfilled mainly through the development of cohesive working relationships with key opinion leaders and regional clinicians of influence. Candidates with varying levels of experience are encouraged to apply. Final title and compensation will be determined based on qualifications and experience. This role will cover the Mid Atlantic region, including SC, NC, VA, MD, Washington DC, and TN. Job Duties and Responsibilities + Identify and engage national, regional, and local oncology thought leaders and HCPs. + Serve as the primary scientific contact and build long-term peer to peer scientific relationships. + Exchange scientific and technical information relevant to the companyu2019s development portfolio. + Support relationships between key opinion leaders and internal product teams. + Educate priority HCPs on research and development initiatives. + Gather medical insightsto inform clinical and marketing strategies. + Provide an overview of company areas of interest for investigator sponsored studies + Contribute to internal educational activities and training. + Represent the company at oncology conferences and scientific meetings. + Lead relevant projects within the field medical organization. Key Core Competencies + Clinical experience or strong scientific research background in oncology/hematology (Prostate Cancer, Myelofibrosis, AML) preferred. + Strong project leadership and time management skills. + Ability to build trust and maintain relationships with thought leaders. + Excellent communication and diplomacy skills. + Understanding of drug development and product lifecycle. + Ability to translate customer needs into actionable insights. + Commitment to continuous improvement and high performance. + Demonstrates a highlycollaborativeapproach to cross-functional engagement, fostering strong partnerships with internal stakeholders and external healthcare professionals. + Applies anagile mindsetto adapt quickly to evolving therapeutic landscapes, scientific data, and organizational priorities. + Values teamworkby contributing to a culture of mutual respect, shared learning, across the medical team. + Exhibits strongself-leadership, proactively managing responsibilities, staying current with scientific developments, and driving personal growth and performance. Travel: >50% Domestic Travel Required Education and Experience + Bacheloru2019s degree in a related fieldrequired.Advanced degree (NP, PA, MD, PharmD, PhD) strongly preferred. + Candidates without an advanced degree must have at least 5 years of MSL experience and 6u201310 years of overall related experience. + MSL experience or relationships with HCPs within the geography preferred. + Generally , an MSL will require : + 5+ years of relevant scientific or clinical experience in oncology/hematology. + Generally , a Sr. MSL will require : + 5+ years of experience in the biotech or pharmaceutical industry. + 3+ years of MSL experience in oncology/hematology. Compensation + MSL : $156,560 u2013 $195,700 + Sr. MSL : $175,680 u2013 $219,600 Final compensation and title will be based on experience and qualifications. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Our robust time-off policy includes flexible paid time off, 11 paid holidays plus additional time off for a shut-down period during the last week of December, 80 hours of paid sick time upon hire and each year thereafter. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education and other factors permitted by law. Disclaimer: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed. Confidential Data : All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential. Compliance : Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of Sumitomo Pharma America (SMPA) and affiliates are carried out with the

Created: 2025-11-01